Sequence of OSGEP_MOUSE
EC Number:2.3.1.234
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
L-threonylcarbamoyladenylate + adenine37 in tRNA = AMP + N6-L-threonylcarbamoyladenine37 in tRNA
Other sequences found for EC No. 2.3.1.234
General information:
Sequence
0 MPAVLGFEGS ANKIGVGVVR DGTVLANPRR TYVTAPGTGF LPGDTARHHR AVILDLLQEA
60 LAEAGLTSKD IDCIAFTKGP GMGAPLASVA VVARTVAQLW NKPLLGVNHC IGHIEMGRLI
120 TGAVNPTVLY VSGGNTQVIS YSEHRYRIFG ETIDIAVGNC LDRFARVLKI SNDPSPGYNI
180 EQMAKRGKKL VELPYTVKGM DVSFSGILSF IEDAAQRMLA TGECTPEDLC FSLQETVFAM
240 LVEITERAMA HCGSKEALIV GGVGCNLRLQ EMMGTMCQER GAQLFATDER FCVDNGAMIA
300 QAGWEMFQAG HRTPLKDSAI TQRYRTDEVE VTWRD
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
70447
Carninci P.,Kasukawa T.,Katayama S.,Gough J.,Frith M.C.,Maeda N.,Oyama R.,Ravasi T.,Lenhard B.,Wells C.,Kodzius R.,Shimokawa K.,Bajic V.B.,Brenner S.E.,Batalov S.,Forrest A.R.,Zavolan M.,Davis M.J.,Wilming L.G.,Aidinis V.,Allen J.E.,Ambesi-Impiombato A.,Apweiler R.,Aturaliya R.N.,Bailey T.L.,Bansal M.,Baxter L.,Beisel K.W.,Bersano T.,Bono H.,Chalk A.M.,Chiu K.P.,Choudhary V.,Christoffels A.,Clutterbuck D.R.,Crowe M.L.,Dalla E.,Dalrymple B.P.,de Bono B.,Della Gatta G.,di Bernardo D.,Down T.,Engstrom P.,Fagiolini M.,Faulkner G.,Fletcher C.F.,Fukushima T.,Furuno M.,Futaki S.,Gariboldi M.,Georgii-Hemming P.,Gingeras T.R.,Gojobori T.,Green R.E.,Gustincich S.,Harbers M.,Hayashi Y.,Hensch T.K.,Hirokawa N.,Hill D.,Huminiecki L.,Iacono M.,Ikeo K.,Iwama A.,Ishikawa T.,Jakt M.,Kanapin A.,Katoh M.,Kawasawa Y.,Kelso J.,Kitamura H.,Kitano H.,Kollias G.,Krishnan S.P.,Kruger A.,Kummerfeld S.K.,Kurochkin I.V.,Lareau L.F.,Lazarevic D.,Lipovich L.,Liu J.,Liuni S.,McWilliam S.,Madan Babu M.,Madera M.,Marchionni L.,Matsuda H.,Matsuzawa S.,Miki H.,Mignone F.,Miyake S.,Morris K.,Mottagui-Tabar S.,Mulder N.,Nakano N.,Nakauchi H.,Ng P.,Nilsson R.,Nishiguchi S.,Nishikawa S.,Nori F.,Ohara O.,Okazaki Y.,Orlando V.,Pang K.C.,Pavan W.J.,Pavesi G.,Pesole G.,Petrovsky N.,Piazza S.,Reed J.,Reid J.F.,Ring B.Z.,Ringwald M.,Rost B.,Ruan Y.,Salzberg S.L.,Sandelin A.,Schneider C.,Schoenbach C.,Sekiguchi K.,Semple C.A.,Seno S.,Sessa L.,Sheng Y.,Shibata Y.,Shimada H.,Shimada K.,Silva D.,Sinclair B.,Sperling S.,Stupka E.,Sugiura K.,Sultana R.,Takenaka Y.,Taki K.,Tammoja K.,Tan S.L.,Tang S.,Taylor M.S.,Tegner J.,Teichmann S.A.,Ueda H.R.,van Nimwegen E.,Verardo R.,Wei C.L.,Yagi K.,Yamanishi H.,Zabarovsky E.,Zhu S.,Zimmer A.,Hide W.,Bult C.,Grimmond S.M.,Teasdale R.D.,Liu E.T.,Brusic V.,Quackenbush J.,Wahlestedt C.,Mattick J.S.,Hume D.A.,Kai C.,Sasaki D.,Tomaru Y.,Fukuda S.,Kanamori-Katayama M.,Suzuki M.,Aoki J.,Arakawa T.,Iida J.,Imamura K.,Itoh M.,Kato T.,Kawaji H.,Kawagashira N.,Kawashima T.,Kojima M.,Kondo S.,Konno H.,Nakano K.,Ninomiya N.,Nishio T.,Okada M.,Plessy C.,Shibata K.,Shiraki T.,Suzuki S.,Tagami M.,Waki K.,Watahiki A.,Okamura-Oho Y.,Suzuki H.,Kawai J.,Hayashizaki Y.
The transcriptional landscape of the mammalian genome.
Science
309
1559-1563
2005
70448
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
70449
Ikeda S.,Ayabe H.,Mori K.,Seki Y.,Seki S.
Identification of the functional elements in the bidirectional promoter of the mouse O-sialoglycoprotein endopeptidase and APEX nuclease genes.
Biochem. Biophys. Res. Commun.
296
785-791
2002
70450
Huttlin E.L.,Jedrychowski M.P.,Elias J.E.,Goswami T.,Rad R.,Beausoleil S.A.,Villen J.,Haas W.,Sowa M.E.,Gygi S.P.
A tissue-specific atlas of mouse protein phosphorylation and expression.
Cell
143
1174-1189
2010
70451
Braun D.A.,Rao J.,Mollet G.,Schapiro D.,Daugeron M.C.,Tan W.,Gribouval O.,Boyer O.,Revy P.,Jobst-Schwan T.,Schmidt J.M.,Lawson J.A.,Schanze D.,Ashraf S.,Ullmann J.F.P.,Hoogstraten C.A.,Boddaert N.,Collinet B.,Martin G.,Liger D.,Lovric S.,Furlano M.,Guerrera I.C.,Sanchez-Ferras O.,Hu J.F.,Boschat A.C.,Sanquer S.,Menten B.,Vergult S.,De Rocker N.,Airik M.,Hermle T.,Shril S.,Widmeier E.,Gee H.Y.,Choi W.I.,Sadowski C.E.,Pabst W.L.,Warejko J.K.,Daga A.,Basta T.,Matejas V.,Scharmann K.,Kienast S.D.,Behnam B.,Beeson B.,Begtrup A.,Bruce M.,Ch'ng G.S.,Lin S.P.,Chang J.H.,Chen C.H.,Cho M.T.,Gaffney P.M.,Gipson P.E.,Hsu C.H.,Kari J.A.,Ke Y.Y.,Kiraly-Borri C.,Lai W.M.,Lemyre E.,Littlejohn R.O.,Masri A.,Moghtaderi M.,Nakamura K.,Ozaltin F.,Praet M.,Prasad C.,Prytula A.,Roeder E.R.,Rump P.,Schnur R.E.,Shiihara T.,Sinha M.D.,Soliman N.A.,Soulami K.,Sweetser D.A.,Tsai W.H.,Tsai J.D.,Topaloglu R.,Vester U.,Viskochil D.H.,Vatanavicharn N.,Waxler J.L.,Wierenga K.J.,Wolf M.T.F.,Wong S.N.,Leidel S.A.,Truglio G.,Dedon P.C.,Poduri A.,Mane S.,Lifton R.P.,Bouchard M.,Kannu P.,Chitayat D.,Magen D.,Callewaert B.,van Tilbeurgh H.,Zenker M.,Antignac C.,Hildebrandt F.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Nat. Genet.
49
1529-1538
2017
